Berberis Homaccord description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Berberis Homaccord

Heel Inc

Berberis Homaccord Oral Drop


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

BERBERIS HOMACCORD INDICATIONS AND USAGE

For the temporary relief of minor:

  • Urinary Pain
  • Urinary Burning

WARNINGS

If you are pregnant or breast feeding, ask a healthcare provider before use. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to Berberis-Homaccord or any of its ingedients exists.

BERBERIS HOMACCORD DOSAGE AND ADMINISTRATION

Directions: Standard Dosage: Adults and children above 12 years and older: 30 drops per day, taking 10 drops every 4 to 6 hours.

Children under 12 years: Consult your healthcare provider.

Initial Dosage: Adults and children 12 years and older: 10 drops every ½ to 1 hour until symptoms lessen, then continue with standard

dosage. Do not exceed 120 drops in 24 hours.

Children under 12 years: Consult your healthcare provider.

ACTIVE INGREDIENT

Each 50ml contains: Active ingredients: *Berberis vulgaris 2X (Final Concentration 4X),10X, 30X, 200X, Colocynthis 3X, 10X, 30X,

200X, *Veratrum album 3X, 10X, 30X 200X

* Natural Ingredients

INACTIVE INGREDIENT

Inactive I ngredients: Ethanol, Purified water

PURPOSE

For the temporary relief of minor: Urinary Pain and Urinary Burning

Berberis Homaccord

Berberis Homaccord

BERBERIS VULGARIS ROOT BARK, CITRULLUS COLOCYNTHIS FRUIT PULP and VERATRUM ALBUM ROOT LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-1200
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK 2 [hp_X]
CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP 3 [hp_X]
VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT 3 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50114-1200-4 50 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1986-01-31


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.